机译:单缝合性颅骨肌肤源:鉴定与综合征形式相关的基因中的罕见变体
Center for Developmental Biology and Regenerative MedicineSeattle Children's Research;
Center for Developmental Biology and Regenerative MedicineSeattle Children's Research;
Center for Developmental Biology and Regenerative MedicineSeattle Children's Research;
Washington University Department of NeurosurgerySt. Louis Missouri;
Center for Developmental Biology and Regenerative MedicineSeattle Children's Research;
Department of Genome SciencesUniversity of WashingtonSeattle Washington;
Department of Genome SciencesUniversity of WashingtonSeattle Washington;
Division of Plastic Surgery Department of SurgeryUniversity of Washington School of;
Seattle Children's Craniofacial CenterSeattle Children's HospitalSeattle Washington;
Seattle Children's Craniofacial CenterSeattle Children's HospitalSeattle Washington;
Division of Plastic Surgery Department of SurgeryUniversity of Washington School of;
Division of Plastic Surgery Department of SurgeryUniversity of Washington School of;
Center for Developmental Biology and Regenerative MedicineSeattle Children's Research;
craniosynostosis; enrichment; gene burden; non syndromic; protein domains; RNA sequencing; single suture; variants;
机译:单缝合性颅骨肌肤源:鉴定与综合征形式相关的基因中的罕见变体
机译:单缝线颅骨融合症的拷贝数变异分析:包括罕见的变异,包括在两个表皮颅突神经症患者中的RUNX2复制。
机译:非综合征性单缝颅骨融合症患者Chiari I型畸形的不对称性
机译:先天性变形和稀有遗传综合征的耳蜗植入:Goldenhar和Branchio-Oculo-Facial
机译:大豆枯萎病病原体(Fusarium virguliforme)的致病性基因的鉴定和表征。
机译:单缝线颅骨融合症:综合征形式相关基因的罕见变异的鉴定。
机译:单线颅骨融合症中的拷贝数变异分析:包括罕见的变异,包括在两个具有同位颅骨融合症的表亲中RUNX2复制